An associate professor of finance at the University of Indianapolis believes Indianapolis-based Eli Lilly and Co. (NYSE: LLY) will be leaner moving forward. Matt Will says Lilly has been cutting expenses in preparation for Wednesday's U.S. patent expiration of its depression medication Cymbalta, which accounted for 22 percent of revenue last year. He says the company hopes decreasing payroll expenses and beefing up research and development will help offset an “obvious” drop in future revenue. Lilly hopes to launch multiple drugs next year, including diabetes and cancer treatments. The company's osteoporosis drug Evista is set to lose patent protection in March 2014.
In October, Lilly outlined its plans to return to revenue growth. The company hopes to generate at least $20 billion in revenue and $3 billion in net income through 2014. The company announced a $700 million investment last month in its fight against global diabetes. The effort includes enhanced insulin production operations in Indianapolis, Puerto Rico, France and China.
Source: Inside INdiana Business
October 3, 2013
INDIANAPOLIS, Ind. – Eli Lilly and Company (NYSE:LLY) expects to launch several new medicines to treat unmet patient needs beginning next year, and return the company to revenue growth and expanding margins after 2014, senior executives told the investment community today at the company's global research and corporate headquarters.
Lilly also reaffirmed its near-term goals of generating at least $20 billion in revenue, $3 billion in net income and $4 billion in operating cash flow through 2014, despite the impending loss of revenue due to patent expirations for two major products in the U.S., beginning in December of this year. The company also announced a new share repurchase program that will return an additional $5 billion to shareholders over time.
The upbeat outlook demonstrates that Lilly has been successfully executing its long-term innovation strategy to weather the significant impact of patent expiries from 2011-2014 and advance more medicines through late-stage development, approval and launch. The company's strategy to focus on development of innovative medicines has produced the strongest pipeline in Lilly's 137-year history, with 13 potential medicines in Phase 3, the final stage of clinical studies, or in regulatory review; and 26 more in Phase 2. This represents a total number in mid-to-late-stage development that is five times greater than the comparable total in 2004.
Launching several of those late-stage molecules will bring new medicines to patients and enable the company to return to revenue growth after 2014, John C. Lechleiter Ph.D., Lilly's chairman, president and chief executive officer, told analysts gathered at the investment event.
“We've undertaken extensive efforts to transform our company to address the challenge of patent expirations and the demands of patients and payers for greater value from medicine,” Lechleiter said. “Today, we're seeing our strategy bear fruit, backed by clinical data that strengthens our confidence in our innovation-based strategy and in our ability to return to growth. We're determined to seize the tremendous opportunities before us and drive a new era of growth for Lilly and its shareholders, while delivering on our mission of improving the lives of patients.”
Specifically, Lilly executives noted several key events this year that demonstrate progress in the company's innovation-based strategy:
U.S. and European regulatory submissions for two medicines to treat type 2 diabetes: empagliflozin (with partner Boehringer Ingelheim) and dulaglutide.
European submission of a new insulin glargine product to treat type 1 and type 2 diabetes.
U.S. and EU regulatory submissions completed for ramucirumab as a single-agent treatment for patients with advanced gastric cancer who have had disease progression after initial chemotherapy.
Second positive Phase III trial of ramucirumab in advanced gastric cancer, with the RAINBOW combination therapy trial demonstrating both improved overall survival and progression-free survival.
Positive results for necitumumab for patients with metastatic squamous non-small cell lung cancer, which could form the basis for a regulatory submission as early as 2014.
In 2014, the company believes it could launch empagliflozin, dulaglutide, and ramucirumab, subject to regulatory approval.
“Lilly has successfully replenished and advanced our pipeline to drive growth post-2014, while building a sustainable R&D engine for the long-term,” said Jan M. Lundberg, Ph.D., executive vice president of science and technology and president of Lilly Research Laboratories. “We've filed for regulatory approval for an unprecedented number of investigational medicines this year with three in diabetes and one in oncology. In the future we expect to maintain a steady state of Phase 3 programs in the mid-to-high single digits, with a robust Phase 1 and Phase 2 pipeline to fill in behind.”
Lundberg noted that in the 2013 – 2014 timeframe, the company expects data readouts or pipeline advancements for nine of the assets in late-stage development. These include the three potential launches noted above, the regulatory submissions of necitumumab and the new insulin glargine product, and new data readouts for four other late-stage assets by the end of 2014. Lundberg also said the company anticipates seeing clinical readouts for the vast majority of its Phase 2 assets during this period.
Chief Financial Officer Derica Rice highlighted the company's strategy to deliver on its financial goals through 2014 and grow revenue and expand margins post-2014.
“To prepare Lilly for 2014 and beyond, we committed to replenishing and advancing our pipeline, driving revenue in our growth engines and key marketed products, and increasing productivity and reducing our cost structure,” Rice said. “We've taken these commitments seriously and made substantial progress toward achieving our near-term goals, and we're confident that this progress positions us for future success.”
Near-term business outlook (through 2014)
In the near-term, Rice said the company still expects to hit its financial goals in 2014, noting:
Selling, general and administrative expenses will decline as the company realizes the full benefit of the restructuring efforts in Europe and the U.S. sales organizations as well as savings from ending the direct-to-consumer promotion of Cymbalta.
The company will realize additional efficiencies in research and development and benefit from a substantial reduction in R&D costs as the pipeline progresses through Phase 3 into regulatory submission.
Rice noted that market factors, including the devaluation of the Yen and slower market growth in key emerging market countries, have moderated the company's near-term revenue growth expectations. These headwinds will make it challenging for the company to meet the minimum revenue goal of $20 billion in 2014, but Rice said the company is focused on finding appropriate ways to achieve this goal. Rice also said the company can and will take additional actions to achieve its 2014 net income and operating cash flow targets through reductions in operating expenses.
“Current consensus for 2014 is in-line with our net income goal, although we may get there in a different way,” Rice said. “For instance, current consensus may underestimate the impact of the Cymbalta and Evista patent expirations on our gross margin percent and our ability to reduce operating expenses, while it may overestimate our tax rate, which is trending in the low 20s percent. As usual, we'll provide specific 2014 line-item guidance in January.”
Medium-term business outlook (post-2014)
Moving beyond 2014, Lilly expects continuing revenue growth in four of its five businesses: Diabetes, Oncol